Are you looking for an exciting career in clinical research? Thermo Fisher Scientific, a global leader in scientific research and drug development, is hiring for multiple roles in India. If you have a background in life sciences, pharmacovigilance, or clinical research, this could be your opportunity to join a world-class contract research organization (CRO).
Current Job Openings at Thermo Fisher Scientific
1. Clinical Research Associate (CRA) – Level I
Job ID: R-01317767
Location: Remote, India
Job Description:
- Ensure essential trial documents comply with ICH-GCP and regulatory requirements.
- Conduct on-site and remote monitoring to verify data accuracy (SDV, SDR, CRF review).
- Track trial progress and maintain study systems (e.g., Clinical Trial Management System).
- Facilitate communication between investigative sites, sponsors, and internal teams.
- Assist in investigator payments, site initiation, and close-out activities.
- Travel to sites as required for monitoring visits.
Qualifications:
- Life Science graduate (required).
- 1+ year of onsite monitoring experience (preferred).
- Strong knowledge of ICH-GCP guidelines.
- Willingness to travel and join immediately.
2. Safety Reporting Coordinator
Job ID: R-01318927
Location: Remote, India
Job Description:
- Provide administrative support for Pharmacovigilance (PV) activities.
- Assist in safety data reconciliation, audits, and regulatory compliance.
- Maintain trial documentation, file organization, and system updates.
- Support PV training and process improvements.
- Coordinate study file distribution and assist in audits.
Qualifications:
- Bachelor’s degree in life sciences, pharmacy, nursing, or related fields.
- Strong organizational and Microsoft Office skills.
- Excellent communication and problem-solving abilities.
- Detail-oriented with the ability to handle multiple tasks.
3. Medical Project Coordinator
Job ID: R-01318933
Location: Remote, India
Job Description:
- Assist in managing medical and safety projects for clinical trials.
- Review safety data trends, coding, and regulatory compliance.
- Support safety management plans and aggregate report reviews.
- Collaborate with clinical/data management teams.
- Present findings in client and investigator meetings.
Qualifications:
- Bachelor’s degree in Nursing, Physician’s Assistant, or related health sciences.
- 2+ years in clinical safety/pharmacovigilance.
- Knowledge of GCP, SAE reporting, and drug safety.
- Strong analytical and communication skills.
Why Join Thermo Fisher Scientific?
- Global Impact: Contribute to life-changing therapies and clinical trials in 100+ countries.
- Career Growth:Â Opportunities for training, mentorship, and professional development.
- Work-Life Balance:Â Flexible remote work options.
- Innovative Culture: Be part of a team driving advancements in pharma and biotech.
How to Apply?
Application Link For Clinical Research Associate (CRA) – Level I
Application Link For Safety Reporting Coordinator
Application Link For Medical Project Coordinator
